A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613636



Internal ID16401045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13936439..13975481hg38UCSC Ensembl
Innerchr9:13936438..13975480hg19UCSC Ensembl
Innerchr9:13926438..13965480hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3839043
hg1939043
hg1839043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128780
Samples
Known GenesLINC00583
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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